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Face processing in 22q11.2 deletion syndrome: atypical development and visual scanning alterations.

Alexandra ZahariaMaude SchneiderBronwyn GlaserMartina FranchiniSarah MenghettiMarie SchaerMartin DebbanéStephan Eliez
Published in: Journal of neurodevelopmental disorders (2018)
The current study brings new evidence of altered face exploration in 22q11.2DS and identifies developmental mechanisms that may contribute to difficulties impacting social interactions in the syndrome.
Keyphrases
  • case report
  • healthcare
  • mental health
  • genome wide
  • dna methylation
  • mass spectrometry